Adaptive deep propagation graph neural network for predicting miRNA–disease associations

Author:

Hu Hua1,Zhao Huan2,Zhong Tangbo2,Dong Xishang1,Wang Lei13,Han Pengyong4,Li Zhengwei135

Affiliation:

1. Zaozhuang University College of Information Science and Engineering, , Zaozhuang 277122 , China

2. China University of Mining and Technology School of Computer Science and Technology, , Xuzhou 221008 , China

3. Guangxi Academy of Science Big Data and Intelligent Computing Research Center, , Nanning 541006 , China

4. Changzhi Medical College Central Lab, , Changzhi 046012 , China

5. KUNPAND Communications (Kunshan) Co., Ltd. , Suzhou 215300 , China

Abstract

Abstract Background A large number of experiments show that the abnormal expression of miRNA is closely related to the occurrence, diagnosis and treatment of diseases. Identifying associations between miRNAs and diseases is important for clinical applications of complex human diseases. However, traditional biological experimental methods and calculation-based methods have many limitations, which lead to the development of more efficient and accurate deep learning methods for predicting miRNA–disease associations. Results In this paper, we propose a novel model on the basis of adaptive deep propagation graph neural network to predict miRNA–disease associations (ADPMDA). We first construct the miRNA–disease heterogeneous graph based on known miRNA–disease pairs, miRNA integrated similarity information, miRNA sequence information and disease similarity information. Then, we project the features of miRNAs and diseases into a low-dimensional space. After that, attention mechanism is utilized to aggregate the local features of central nodes. In particular, an adaptive deep propagation graph neural network is employed to learn the embedding of nodes, which can adaptively adjust the local and global information of nodes. Finally, the multi-layer perceptron is leveraged to score miRNA–disease pairs. Conclusion Experiments on human microRNA disease database v3.0 dataset show that ADPMDA achieves the mean AUC value of 94.75% under 5-fold cross-validation. We further conduct case studies on the esophageal neoplasm, lung neoplasms and lymphoma to confirm the effectiveness of our proposed model, and 49, 49, 47 of the top 50 predicted miRNAs associated with these diseases are confirmed, respectively. These results demonstrate the effectiveness and superiority of our model in predicting miRNA–disease associations.

Funder

Changzhi Medical College Startup Fund for PhD faculty

Shanxi Province Science Foundation for Youths

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Genetics,Molecular Biology,Biochemistry,General Medicine

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